FDAnews Device Daily Bulletin
May 7, 2012
| Vol.
9 No.
90
Lax documentation of testing failures and inadequate design history files for Novalung’s surgical Lung Assist device have earned the German company an FDA warning letter.
The European Commission is preparing guidance to assist notified bodies during inspections of facilities where CE-marked medical devices are made.
Pioneer Surgical has issued a field safety notice for its Nubac Trial Inserter – 43-TRL-INSERTER.
The grass is greener on the other side.
The Massachusetts House of Representatives recently voted on and passed its proposals for the commonwealth’s Fiscal 2013 budget.
Kensey Nash will be acquired by Royal DSM for $360 million.
Each prescription drug you take has a unique code that the government can use to track problems.
Andrew Technologies launched the HydraSolve Lipoplasty System at the American Society of Aesthetic Plastic Surgery in Vancouver, BC.
Avanquest Software has developed an app that may save lives during emergency situations.
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